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Results: 1 to 14 of 14

Tests names and labsConditionsGenes, analytes, and microbesMethods

LIPI Gene Hypertriglyceridemia, susceptibility to NGS Genetic DNA Test

DNA Labs India
India
11
  • S Mutation scanning of the entire coding region

CentoMetabolic MOx

Centogene AG - the Rare Disease Company
Germany
195221
  • A Analyte
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Hypertriglyceridemia, susceptibility to, 145750, Autosomal dominant (LIPI gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Dyslipidemia (WES based NGS panel of 25 genes, including CNV analysis)

CGC Genetics Unilabs
Portugal
125
  • C Sequence analysis of the entire coding region

Hyperlipoproteinemia type 4 (sequence analysis of LIPI gene)

CGC Genetics Unilabs
Portugal
11
  • C Sequence analysis of the entire coding region

Familial Hypertriglyceridemia NGS Panel

Fulgent Genetics
United States
2015
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

MAJOR HYPERTRIGLYCERIDEMIA SANGER PANEL

Laboratorio de Genetica Clinica SL
Spain
16
  • C Sequence analysis of the entire coding region

HYPERLIPOPROTEINEMIA TYPE 4

Laboratorio de Genetica Clinica SL
Spain
11
  • C Sequence analysis of the entire coding region

Major Hypertriglyceridemia, Panel Massive Sequencing (NGS) 7 Genes

Reference Laboratory Genetics
Spain
67
  • C Sequence analysis of the entire coding region

MAJOR HYPERTRIGLYCERIDEMIA

Laboratorio de Genetica Clinica SL
Spain
56
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Major Hypertriglyceridemia, Sequencing LIPI Gene

Reference Laboratory Genetics
Spain
11
  • C Sequence analysis of the entire coding region

Familial hypertriglyceridemia

Bioarray
Spain
11
  • C Sequence analysis of the entire coding region

LIPI Single Gene

Fulgent Genetics
United States
11
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Clinical Exome

Fulgent Genetics
United States
51294672
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Results: 1 to 14 of 14

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.